This training on Adverse Event Reporting in Clinical Trials will show how to accurately observe and report AEs and SAEs, avoid common mistakes in AE /SAE reporting and successfully clear an FDA audit.
This 3-hr virtual seminar will discuss the requirements and compliance in medical device adverse event reporting and medical device surveillance/vigilance system in the US, Europe and Canada.
Download events tagged adverse event reporting in XML or iCalendar format.
The Boxes and Arrows event calendar is a place to find events of interest to designers. These can be specific design events, such as an AIGA event, SXSW or the IA Summit, part design/part other, such as Webvisions or it can be tangentially related, such as a business event or one on CSS.
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